Lnx2 Variant Search Result - Rat Genome Database

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70 records found for search term Lnx2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8582734	CV117290	single nucleotide variant	NM_153371.3(LNX2):c.-100-2396G>C	Lung cancer [RCV000097811]	uncertain significance	13	27584199	27584199	Human		name
405810124	CV3283919	single nucleotide variant	NM_153371.4(LNX2):c.10A>G (p.Thr4Ala)	not specified [RCV004407839]	uncertain significance	13	27581694	27581694	Human		name
405810316	CV3283927	single nucleotide variant	NM_153371.4(LNX2):c.408A>G (p.Arg136=)	not specified [RCV004407847]	likely benign	13	27569276	27569276	Human		name
155937979	CV2364949	single nucleotide variant	NM_153371.4(LNX2):c.262C>T (p.Arg88Trp)	not specified [RCV004222243]	uncertain significance	13	27581442	27581442	Human		name
329369543	CV2461151	single nucleotide variant	NM_153371.4(LNX2):c.224G>A (p.Arg75Lys)	not specified [RCV004265566]	uncertain significance	13	27581480	27581480	Human		name
405810324	CV3283923	single nucleotide variant	NM_153371.4(LNX2):c.188C>T (p.Thr63Ile)	not specified [RCV004407843]	uncertain significance	13	27581516	27581516	Human		name
405810318	CV3283926	single nucleotide variant	NM_153371.4(LNX2):c.236A>G (p.Gln79Arg)	not specified [RCV004407846]	uncertain significance	13	27581468	27581468	Human		name
597623325	CV3701846	single nucleotide variant	NM_153371.4(LNX2):c.1938G>A (p.Lys646=)	not specified [RCV004936356]	likely benign	13	27548470	27548470	Human		name
598238457	CV3991718	single nucleotide variant	NM_153371.4(LNX2):c.196G>A (p.Gly66Arg)	not specified [RCV005364252]	uncertain significance	13	27581508	27581508	Human		name
15199857	CV702646	single nucleotide variant	NM_153371.4(LNX2):c.1446C>T (p.Thr482=)	not provided [RCV000957161]	benign	13	27556336	27556336	Human		name
156250643	CV2196323	single nucleotide variant	NM_153371.4(LNX2):c.656C>T (p.Thr219Ile)	not specified [RCV004072501]	uncertain significance	13	27567839	27567839	Human		name
155922964	CV2251815	single nucleotide variant	NM_153371.4(LNX2):c.956G>A (p.Arg319His)	not specified [RCV004119804]	uncertain significance	13	27562681	27562681	Human		name
156004088	CV2290106	single nucleotide variant	NM_153371.4(LNX2):c.613G>A (p.Gly205Ser)	not specified [RCV004152782]	uncertain significance	13	27569071	27569071	Human		name
156156749	CV2314403	single nucleotide variant	NM_153371.4(LNX2):c.475A>G (p.Ile159Val)	not specified [RCV004168521]	uncertain significance	13	27569209	27569209	Human		name
155966517	CV2329808	single nucleotide variant	NM_153371.4(LNX2):c.587C>T (p.Ser196Phe)	not specified [RCV004183273]	uncertain significance	13	27569097	27569097	Human		name
156277681	CV2330856	single nucleotide variant	NM_153371.4(LNX2):c.509C>T (p.Pro170Leu)	not specified [RCV004185911]	likely benign	13	27569175	27569175	Human		name
155923743	CV2347557	single nucleotide variant	NM_153371.4(LNX2):c.541T>G (p.Leu181Val)	not specified [RCV004200496]	uncertain significance	13	27569143	27569143	Human		name
329393966	CV2449995	single nucleotide variant	NM_153371.4(LNX2):c.959T>G (p.Phe320Cys)	not specified [RCV004269057]	uncertain significance	13	27562678	27562678	Human		name
401773128	CV2698103	single nucleotide variant	NM_153371.4(LNX2):c.617T>G (p.Leu206Arg)	not specified [RCV004302894]	uncertain significance	13	27569067	27569067	Human		name
405810314	CV3283928	single nucleotide variant	NM_153371.4(LNX2):c.589C>T (p.Leu197Phe)	not specified [RCV004407848]	uncertain significance	13	27569095	27569095	Human		name
405810311	CV3283929	single nucleotide variant	NM_153371.4(LNX2):c.698C>T (p.Thr233Met)	not specified [RCV004407849]	uncertain significance	13	27567797	27567797	Human		name
405810309	CV3283930	single nucleotide variant	NM_153371.4(LNX2):c.803A>G (p.Asp268Gly)	not specified [RCV004407850]	uncertain significance	13	27567692	27567692	Human		name
405810307	CV3283931	single nucleotide variant	NM_153371.4(LNX2):c.878A>G (p.Asn293Ser)	not specified [RCV004407851]	uncertain significance	13	27562759	27562759	Human		name
405810305	CV3283932	single nucleotide variant	NM_153371.4(LNX2):c.913C>G (p.Gln305Glu)	not specified [RCV004407852]	uncertain significance	13	27562724	27562724	Human		name
407461174	CV3445832	single nucleotide variant	NM_153371.4(LNX2):c.610C>T (p.Pro204Ser)	not specified [RCV004634060]	uncertain significance	13	27569074	27569074	Human		name
407471557	CV3445835	single nucleotide variant	NM_153371.4(LNX2):c.334G>C (p.Val112Leu)	not specified [RCV004637317]	uncertain significance	13	27581370	27581370	Human		name
407471548	CV3445837	single nucleotide variant	NM_153371.4(LNX2):c.428G>A (p.Arg143Gln)	not specified [RCV004637319]	uncertain significance	13	27569256	27569256	Human		name
597623323	CV3701843	single nucleotide variant	NM_153371.4(LNX2):c.643G>A (p.Ala215Thr)	not specified [RCV004936354]	uncertain significance	13	27569041	27569041	Human		name
597623326	CV3701847	single nucleotide variant	NM_153371.4(LNX2):c.676T>G (p.Leu226Val)	not specified [RCV004936357]	uncertain significance	13	27567819	27567819	Human		name
597623327	CV3701848	single nucleotide variant	NM_153371.4(LNX2):c.634G>A (p.Glu212Lys)	not specified [RCV004936358]	uncertain significance	13	27569050	27569050	Human		name
597623329	CV3701850	single nucleotide variant	NM_153371.4(LNX2):c.361A>G (p.Lys121Glu)	not specified [RCV004936360]	uncertain significance	13	27581343	27581343	Human		name
597623331	CV3701852	single nucleotide variant	NM_153371.4(LNX2):c.367G>A (p.Val123Ile)	not specified [RCV004936362]	uncertain significance	13	27581337	27581337	Human		name
597796019	CV3701854	single nucleotide variant	NM_153371.4(LNX2):c.341G>A (p.Cys114Tyr)	not specified [RCV004935074]	uncertain significance	13	27581363	27581363	Human		name
597623334	CV3701856	single nucleotide variant	NM_153371.4(LNX2):c.947G>A (p.Arg316Gln)	not specified [RCV004936365]	uncertain significance	13	27562690	27562690	Human		name
597623335	CV3701857	single nucleotide variant	NM_153371.4(LNX2):c.457A>G (p.Ser153Gly)	not specified [RCV004936366]	uncertain significance	13	27569227	27569227	Human		name
156381696	CV2212314	single nucleotide variant	NM_153371.4(LNX2):c.1114G>T (p.Gly372Trp)	not specified [RCV004091264]	uncertain significance	13	27562523	27562523	Human		name
156291020	CV2306019	single nucleotide variant	NM_153371.4(LNX2):c.1223A>G (p.Gln408Arg)	not specified [RCV004161002]	uncertain significance	13	27562414	27562414	Human		name
156094881	CV2310050	single nucleotide variant	NM_153371.4(LNX2):c.1165G>A (p.Ala389Thr)	not specified [RCV004163183]	uncertain significance	13	27562472	27562472	Human		name
156275206	CV2318231	single nucleotide variant	NM_153371.4(LNX2):c.1837T>C (p.Phe613Leu)	not specified [RCV004179415]	uncertain significance	13	27550433	27550433	Human		name
156071535	CV2325221	single nucleotide variant	NM_153371.4(LNX2):c.1080T>G (p.Asp360Glu)	not specified [RCV004177630]	uncertain significance	13	27562557	27562557	Human		name
156150872	CV2394684	single nucleotide variant	NM_153371.4(LNX2):c.1179C>A (p.His393Gln)	not specified [RCV004234366]	uncertain significance	13	27562458	27562458	Human		name
329375520	CV2431550	single nucleotide variant	NM_153371.4(LNX2):c.1289T>C (p.Ile430Thr)	not specified [RCV004254703]	uncertain significance	13	27559921	27559921	Human		name
329372960	CV2434053	single nucleotide variant	NM_153371.4(LNX2):c.1363C>T (p.His455Tyr)	not specified [RCV004249953]	uncertain significance	13	27559847	27559847	Human		name
329393279	CV2449620	single nucleotide variant	NM_153371.4(LNX2):c.1999C>G (p.Leu667Val)	not specified [RCV004268538]	uncertain significance	13	27548409	27548409	Human		name
401782641	CV2697136	single nucleotide variant	NM_153371.4(LNX2):c.1439G>A (p.Gly480Asp)	not specified [RCV004302131]	uncertain significance	13	27556343	27556343	Human		name
401759935	CV2698680	single nucleotide variant	NM_153371.4(LNX2):c.1543A>G (p.Arg515Gly)	not specified [RCV004301146]	uncertain significance	13	27556239	27556239	Human		name
401719632	CV2701209	single nucleotide variant	NM_153371.4(LNX2):c.1927G>A (p.Gly643Arg)	not specified [RCV004309783]	uncertain significance	13	27550343	27550343	Human		name
401762871	CV2707304	single nucleotide variant	NM_153371.4(LNX2):c.1250C>T (p.Thr417Ile)	not specified [RCV004312710]	uncertain significance	13	27559960	27559960	Human		name
401877145	CV2764511	single nucleotide variant	NM_153371.4(LNX2):c.1988G>A (p.Ser663Asn)	not specified [RCV004339069]	uncertain significance	13	27548420	27548420	Human		name
401893973	CV2770174	single nucleotide variant	NM_153371.4(LNX2):c.1249A>G (p.Thr417Ala)	not specified [RCV004356068]	uncertain significance	13	27559961	27559961	Human		name
405810126	CV3283920	single nucleotide variant	NM_153371.4(LNX2):c.1141C>G (p.Leu381Val)	not specified [RCV004407840]	uncertain significance	13	27562496	27562496	Human		name
405810128	CV3283921	single nucleotide variant	NM_153371.4(LNX2):c.1151A>G (p.Asn384Ser)	not specified [RCV004407841]	uncertain significance	13	27562486	27562486	Human		name
405810326	CV3283922	single nucleotide variant	NM_153371.4(LNX2):c.1734T>G (p.Asp578Glu)	not specified [RCV004407842]	uncertain significance	13	27553252	27553252	Human		name
405810322	CV3283924	single nucleotide variant	NM_153371.4(LNX2):c.1985T>G (p.Met662Arg)	not specified [RCV004407844]	uncertain significance	13	27548423	27548423	Human		name
405810320	CV3283925	single nucleotide variant	NM_153371.4(LNX2):c.2002G>A (p.Val668Ile)	not specified [RCV004407845]	uncertain significance	13	27548406	27548406	Human		name
407471566	CV3445833	single nucleotide variant	NM_153371.4(LNX2):c.1631C>T (p.Ala544Val)	not specified [RCV004637315]	uncertain significance	13	27553355	27553355	Human		name
407471562	CV3445834	single nucleotide variant	NM_153371.4(LNX2):c.1759A>G (p.Met587Val)	not specified [RCV004637316]	uncertain significance	13	27553227	27553227	Human		name
407471552	CV3445836	single nucleotide variant	NM_153371.4(LNX2):c.1313G>T (p.Ser438Ile)	not specified [RCV004637318]	uncertain significance	13	27559897	27559897	Human		name
407471543	CV3445838	single nucleotide variant	NM_153371.4(LNX2):c.1510C>T (p.His504Tyr)	not specified [RCV004637320]	uncertain significance	13	27556272	27556272	Human		name
597623324	CV3701844	single nucleotide variant	NM_153371.4(LNX2):c.1652A>G (p.Lys551Arg)	not specified [RCV004936355]	uncertain significance	13	27553334	27553334	Human		name
597796016	CV3701845	single nucleotide variant	NM_153371.4(LNX2):c.1693G>T (p.Ala565Ser)	not specified [RCV004935073]	uncertain significance	13	27553293	27553293	Human		name
597623328	CV3701849	single nucleotide variant	NM_153371.4(LNX2):c.1117G>T (p.Gly373Trp)	not specified [RCV004936359]	uncertain significance	13	27562520	27562520	Human		name
597623330	CV3701851	single nucleotide variant	NM_153371.4(LNX2):c.1001G>A (p.Arg334Gln)	not specified [RCV004936361]	uncertain significance	13	27562636	27562636	Human		name
597623332	CV3701853	single nucleotide variant	NM_153371.4(LNX2):c.1715T>G (p.Phe572Cys)	not specified [RCV004936363]	uncertain significance	13	27553271	27553271	Human		name
597623333	CV3701855	single nucleotide variant	NM_153371.4(LNX2):c.1811G>A (p.Arg604Gln)	not specified [RCV004936364]	uncertain significance	13	27550459	27550459	Human		name
597623336	CV3701858	single nucleotide variant	NM_153371.4(LNX2):c.1214A>G (p.Gln405Arg)	not specified [RCV004936367]	uncertain significance	13	27562423	27562423	Human		name
598261333	CV3991719	single nucleotide variant	NM_153371.4(LNX2):c.1252A>G (p.Ile418Val)	not specified [RCV005347818]	uncertain significance	13	27559958	27559958	Human		name
598238463	CV3991720	single nucleotide variant	NM_153371.4(LNX2):c.1115G>C (p.Gly372Ala)	not specified [RCV005364253]	uncertain significance	13	27562522	27562522	Human		name
598238469	CV3991721	single nucleotide variant	NM_153371.4(LNX2):c.1736C>T (p.Ala579Val)	not specified [RCV005364254]	uncertain significance	13	27553250	27553250	Human		name
598238475	CV3991722	single nucleotide variant	NM_153371.4(LNX2):c.1655C>T (p.Ala552Val)	not specified [RCV005364255]	uncertain significance	13	27553331	27553331	Human		name

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